No abstract available.
Alloxan* ; Animals ; Rats*

Cataracts often occur in diabetic patients or as a consequence of diabetes experimentally induced with alloxan or streptozotocin. In mammals, the transparency of the lens depends on its Ca++ level, and many researchers have proven experimentally that cataracts may occur in cases of increased lens calcium level. In 1981 Fleckenstein et al. were the first to demonstrate experimentally that the cause of cataracts in the alloxan induced diabetic rat is due to an increased lens calcium level, and this calcium induced cataract may be suppressed by the calcium channel blocker-verapamil which prevents lenticular calcium overload. However, they did not determine the mechanism of verapamif on the inhibitory action of lenticular calcium overload. In this experiment verapamil was administrated to control rats and to streptozotocin induced diabetic rats to discover by what mechanism verapamil prevents the occurrence of cataracts as a complication in experimental diabetic rats. The authors compared lens calcium level and measured active 45Ca efflux from the lens, Na+ - Ca++ exchange and Ca++ - ATPase activity in the lens between the control and experimental groups. Their conclusions are as follows: 1. The calcium level of the lens was significantly increased in SDR(Streptozotocin injected diabetic rat) as compared to NDC(Nondiabetic control rat), VNDC(Verapamil treated nondiabetic control rat) and SVDR(Streptozotocin injected verapamil treated diabetic rat). 2. Active 45Ca efflux across the lens membrane was significantly decreased in SDR as compared to NDC, VNDC and SVDR. 3. The Ca++ - ATPase activity was significantly suppressed in SDR as compared to NDC, VNDC and SVDR. 4. Verapamil had no influence on the Na+ - Ca++ exchange transport system in all groups of NDC, VNDC, SDR and SVDR. Thus, our results suggest that verapamil prevents the occurrence of cataracts in diabetic rats probably by controlling the Ca++ transport system in the lens membrane.
Adenosine Triphosphatases ; Alloxan ; Animals ; Calcium Channels ; Calcium* ; Cataract ; Humans ; Mammals ; Membranes ; Rats* ; Streptozocin ; Verapamil*

The approach and novelty of this scientific work was to formulate the appropriate Streptozotocin (STZ) and Alloxan dosage in different routes of administration to imply minimum mortality rate and high incidence of diabetes mellitus (DM) in the rat experiment model. Rats were randomly divided into STZ, Alloxan and control groups. 1-Alloxan group was divided into two subgroups: intraperitoneal (ip) subgroups which received a single dose of, 140, 120, 100 and 80 mg/kg; and the subcutaneous (sc) subgroups which received a single dose of, 120, 110, 100, 90, and 80 mg/kg. 2-STZ group was divided into four subgroups of ip route. The ip subgroup which received intraperitoneally a single dose of, 30, 35, 40 and 50 mg/kg. 3-The control group: This group received solo distilled water. The injection day was considered as the day zero. Blood glucose levels and mortality rate were recorded. Subsequently, 30 days after, the logistic regression modeling was used to evaluate the effect of the explanatory variables, the dose levels, and route approaches, on the probability of DM incidence, and mortality. According to the statistical logistic analysis for Alloxan, it is concluded that the minimum dosage needed to induce DM was 120 mg/kg by sc method (probability 0.712). In addition, the logistic analysis for STZ showed that the optimal dose-level for STZ was 40 mg/kg with ip with approximate induction of DM probability 0.764. Based on the data, male Wistar rats in which received a single dosage of Alloxan by sc injection at dose of 120 mg/kg showed the most desirable result of induction of type I DM; furthermore, those in which received STZ by ip injection at the dose of 40 mg/kg developed a persistent and optimal DM state characterized by high rate of DM induction and low- level of mortality.
Alloxan* ; Animals ; Blood Glucose ; Diabetes Mellitus* ; Humans ; Incidence ; Logistic Models ; Male ; Methods ; Mortality* ; Rats* ; Rats, Wistar ; Streptozocin* ; Water

This experiment was aimed to investigate the contractile responses of the fermoral artery to the electrical stimulation and the inhibitory effects of verapamil and papaverine on the electrical stimulation of the fermoral artery in the control (n=46) and the diabetic rabbits(n=40). Diabetic rabbits were made by and administration of alloxan (100 mg/kg) intravenously and sacrified 8 weeks later. Femoral arterial rings 3 mm in length were taken and mounted on the force-displacement transducer for the measurements of isometric tension. All experiments were done in the aerated (95% O2 with 5% CO2)biological chamber filled with Kreb's solution and the initial tension of 1.5g was applied to the rings. After 1 hour of equilibrium of the rings, the contractile responses of the electrical stimulation on the femoral arterial rings were taken without vasoactive drugs and then, under verapamil and papaverine solution. And we compared the morphologic findings of the vessels in the two groups in relation to the functional changes by transmission electron miroscopy. The results are as follows: 1. The contractile responses in the presence of verapamil or papaverine solutions to the electrical stimulation were lowed significantly in the fermoral arterial rings of the diabetic rabbits compared with that of the control rabbits (verapamil; 10M~10M: p<0.01, papaverine; 10M & 10M: p<0.01). 2. Transmission electron microphotographs showed many morphological differences of the femoral arteries between the control and the diabetic rabbits. These were irregularities of the internal elastic lamina and the hypertrophy of the cytoplasms of the smooth muscle cells. And also, there were many vacuoles in the cytoplasm of the endothelial cells, lateral to the internal elastic laminaes, and between the smooth muscle cells in the diabetic rabbit femoral artery. By this study, we found that the contractile responses of the femoral arterial rings to the electrical stimulation were decreased in the diabetic rabbits, and the vasodiatory effects of verapamil and papaverine on the electrically stimulated femoral arterial rings were also lowered in the diabetic rabbits compared with the control rabbits. These changes of the vasular responses of the diabetic vessel may be associated with morphological changes manifested by transmission electron microscopy or any other functional derangement of the vessels.
Alloxan ; Arteries ; Cytoplasm ; Electric Stimulation* ; Endothelial Cells ; Femoral Artery ; Hypertrophy ; Microscopy, Electron, Transmission ; Myocytes, Smooth Muscle ; Papaverine ; Rabbits ; Transducers ; Vacuoles ; Vasodilator Agents* ; Verapamil

Alloxan administration in rats is used as a model for non-insulin dependent diabetes mellitus (NIDDM). NIDDM is a multifactorial disease, characterized by hyperglycemia and lipoprotein abnormalities. In this study, we evaluated the antihyperglycemic and antihyperlipidemic effects of fermented Rhynchosia nulubilis (FRN) through the regulation of glucose uptake in alloxan-induced rats. Fermented R. nulubilis was administered orally for 28 d at 500 mg/kg of body weight. Body weight and food intake were monitored every day. Biochemical parameters were quantified after 4 week. In the diabetic + FRN group, body weight increased significantly and blood glucose concentrations decreased when compared to those of the diabetic group. After 2 hr of administration, the oral glucose tolerance test (OGTT) indicated a significant reduction in the diabetic + FRN group compared to diabetic group. The diabetic + FRN group experienced a significant reduction in total cholesterol, triglycerides, low density lipoprotein, coronary risk factors, and malondialdehyde concentrations, with significantly increased high density lipoprotein compared to those of diabetic group. These results demonstrate that fermented R. nulubilis possesses potent antihyperglycemic and antihyperlipidemic activity in alloxan-induced diabetic rats.
Alloxan ; Animals ; Blood Glucose ; Body Weight ; Cholesterol ; Diabetes Mellitus ; Diabetes Mellitus, Type 2 ; Eating ; Glucose ; Glucose Tolerance Test ; Hyperglycemia ; Lipoproteins ; Malondialdehyde ; Rats ; Risk Factors ; Triglycerides

The effect of alloxan-diabetic rat fed with normal, high fat, low protein and high protein diets on the rate of urea production and the activities of enzymes associated with the urea cycle (ornithine transcarbamoylase, E.C. 2.1.3.3, OTC; arginase, E.C. 3.5.5.1) have been studied in intact and isolated perfused liver. The amount of urea excretion was the highest in the high protein diet group. When each diet group was treated with alloxan, total urea excretion showed little differences between each diet group and its corresponding control group with the exception being in the normal diet group. However, the enzyme activity of OTC was increased significantly by alloxan treatment in low and high protein diet groups as compared to corresponding control groups. Similar results were obtained in arginase activity, although the magnitude of the change was less marked. In liver perfusion experiments on rats treated with alloxan, the amount of urea production and changes in OTC and arginase activity were very similar with those in the intact liver. These results suggest that alloxan treatment in normal diet group causes an increase in urea excretion both in intact and perfused liver regardless of changes in enzyme activities and total urea excretion, and enzyme activities are affected by changes in dietary components but the changes of enzyme activities may not correlate with total urea excretion.
Alloxan ; Animal ; Diabetes Mellitus, Experimental/metabolism* ; Dietary Fats/pharmacology* ; Dietary Proteins/pharmacology* ; In Vitro ; Liver/metabolism* ; Male ; Perfusion ; Rats ; Urea/metabolism* ; Urea/urine

PURPOSE: Diabetic women commonly reported decreased sexual arousal and a lack of vaginal lubrication. Genital arousal depends on the vaginal blood flow and the vaginal smooth muscle tone. The aim of this study was to investigate the effect of diabetes mellitus on the relaxation of the vaginal smooth muscles in the rabbit models. MATERIALS AND METHODS: New Zealand White female rabbits (3-3.5kg) were divided into two groups: control (n=5) and experimental (n=20). The experimental group received an intravenous injection of alloxan (100mg/kg). The development of diabetes was verified by measuring the body weight and blood glucose levels. After 12 weeks, the reactivity of the vaginal tissue from the control and diabetic animals was studied examined in the organ chambers. Vaginal The vaginal tissue was also processed immunohistochemically to determine the presence of the neuronal NOS isoform (n-NOS) in similar groups of rabbits. RESULTS: By After 12 weeks, five 5 of the 20 animals developed diabetes mellitus. The mean blood glucose level was significantly increased higher in the experimental group (340.8+/-116.9 mg/dl) compared to the control group (81.3+/-6.2mg/dl) (p=0.004). There was no significant difference in terms of the rRelaxation of vaginal tissue to electrical stimulation of the autonomic nerves, to the endothelium-dependent vasodilator acetylcholine and to the endothelium-independent vasodilator nitroprruside was not significantly different between the control and diabetic group. n-NOS immunoreactivity was also similar in both the control and diabetic groups. CONCLUSIONS: This The results suggest that diabetes mellitus may does not impair the neurogenic and endothelium-dependent relaxation of the rabbit vaginal smooth muscle. However, further intensive studies areinvestigation is needed to verify these results.
Acetylcholine ; Alloxan ; Animals ; Arousal ; Autonomic Pathways ; Blood Glucose ; Body Weight ; Diabetes Mellitus* ; Electric Stimulation ; Female ; Humans ; Injections, Intravenous ; Lubrication ; Muscle, Smooth* ; Neurons ; New Zealand ; Rabbits ; Relaxation* ; Vagina

PURPOSE: The purpose of this study was to evaluate the optimal diabetes duration for bone regeneration experiments in an alloxan monohydrate (ALX)–induced diabetic rabbit calvarial defect model by evaluating the association between diabetes duration and bone healing capacity. METHODS: Twenty-four New Zealand white rabbits were used. Twenty-two rabbits were injected with 100 mg/kg of ALX to induce experimental diabetes. These rabbits were divided into 4 groups, including a control group and groups with diabetes durations of 1 week (group 1), 2 weeks (group 2), and 4 weeks (group 3). Calvarial defects were created at 1, 2, and 4 weeks after ALX injection and in the control rabbits. Cone-beam computed tomography (CBCT) scanning was performed on the day of surgery and at 2 and 4 weeks after surgery. The rabbits were sacrificed 4 weeks after surgery, followed by histological and immunofluorescence analysis. RESULTS: The diabetic state of all diabetic rabbits was well-maintained throughout the experiment. Reconstructed 3-dimensional CBCT imaging showed more rapid and prominent bone regeneration in the control group than in the experimental groups. Histological staining showed notable bone regeneration in the control group, in contrast to scarce bone formation in the experimental groups. The appearance and immunoreactivity of receptor activator of nuclear factor-kappa B and osteoprotegerin did not show notable differences among the groups. CONCLUSION: ALX administration at 100 mg/kg successfully induced experimental diabetes in rabbits. The effect of diabetes on bone healing was evident when the interval between diabetes induction and the intervention was ≥1 week.
Alloxan ; Animals ; Bone Regeneration ; Cone-Beam Computed Tomography ; Diabetes Mellitus, Experimental ; Fluorescent Antibody Technique ; Osteogenesis ; Osteoprotegerin ; Rabbits ; Receptor Activator of Nuclear Factor-kappa B

Objective To establish a Daphnia model of alloxan-induced diabetes. Methods Daphnia were exposed to three different concentrations of alloxan (3, 5, and 10 mmol/L) for 30 minutes. Blood glucose and survival rate were recorded for 72 hours after alloxan insult. Sequence analysis and phylogenetic inference for glucose transporters (GLUT) were clustered with the maximum-likelihood method. Using reverse transcription and quantitative polymerase chain reaction techniques, we investigated the transcriptional changes of GLUT at 12 hours after alloxan (5 mmol/L) exposure. Results Compared with control, 3 mmol/L, and 5 mmol/L as well as 10 mmol/L alloxan initially induced transient blood glucose decline by 15% for 2 hours and 12 hours respectively. In Daphnia with 5 and 10 mmol/L alloxan, their blood glucose was persistently raised by about 150% since after 24-hour insult. Survival rate of Daphnia exposure to alloxan with concentrations of 3, 5, and 10 mmol/L were 90%, 75%, and 25% respectively. We predicted seven GLUT genes in the Daphnia genome and successfully amplified them using real-time polymerase chain reaction. Two of seven GLUT transcripts were down-regulated in Daphnia with 5 mmol/L alloxan-induced diabetes. Conclusion Alloxan-induced diabetes model was successfully established in the Daphnia pulex, suggesting diabetes-relevant experiments can be conducted using Daphnia.
Alloxan ; Animals ; Blood Glucose ; analysis ; Daphnia ; Diabetes Mellitus, Experimental ; chemically induced ; physiopathology ; Disease Models, Animal ; Gene Expression Regulation ; Glucose Transport Proteins, Facilitative ; genetics ; metabolism ; Likelihood Functions ; Phylogeny ; Real-Time Polymerase Chain Reaction

OBJECTIVETo investigate the effect of Musa sapientum L. (MS) bark juice in diabetic gastroparesis and its effect on pharmacokinetic of metformin (MET).

METHODSDiabetes was induced in rats by administering alloxan (120 mg/kg) saline solution and maintained for 8 week. All the 18 Sprague-Dawley rats were divided into three groups (n =6 in each group): normal control, diabetic control and MS bark juice. Assessment of diabetes was done by glucose oxidase-peroxidase method on the 3rd day of alloxan administration. The effects of MS bark juice (100 mL/kg) on gastric emptying time, intestinal transit time, contractility of fundus and pylorus as well as gastric acid secretion in chronic diabetic rats were observed after 8 weeks of alloxan administration. The effect of MS bark juice on the pharmacokinetic of orally administered single dose of MET (350 mg/kg) was evaluated on the 57th day of protocol. Any drugs that may reduce the blood glucose level or influence the fibrinolytic system were not used in this study.

RESULTSThe MS bark juice significantly reduced the blood glucose level in the diabetic rats (P<0.01). There was significant decrease in the pylorus motility and increase in the gastric emptying time, intestinal transit time, contractility of fundus, gastric acid secretion in the MS bark juice treated group (P<0.01). There was significant decrease in the time at which drug at a maximum concentration, half life of drug and increase in the maximum concentration of drug in the plasma of MET in MS bark juice treated group as compared to diabetic control group (P<0.01).

CONCLUSIONMS bark juice effectively manages diabetic gastroparesis and thereby improves the bioavailabilty of MET when administered with MS bark juice.

Alloxan ; Animals ; Blood Glucose ; Chromatography, High Pressure Liquid ; Diabetes Mellitus, Experimental ; blood ; complications ; drug therapy ; physiopathology ; Gastroparesis ; blood ; complications ; drug therapy ; physiopathology ; Male ; Metformin ; blood ; pharmacokinetics ; therapeutic use ; Musa ; chemistry ; Plant Extracts ; pharmacology ; therapeutic use ; Rats, Sprague-Dawley